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Fetal and neonatal alloimmune thrombocytopenia
6 associated genes
No signs/symptoms info
PROTEIN INTERACTIONS: 2
Familial renal amyloidosis due to fibrinogen A alpha-chain variant
1 associated gene
No signs/symptoms info
Fetal and neonatal alloimmune thrombocytopenia
Familial renal amyloidosis due to fibrinogen A alpha-chain variant

CD109
(UniProt - OMIM)
 FGA
(UniProt - OMIM)
GP1BA
(UniProt - OMIM)
GP1BB
(UniProt - OMIM)
ITGA2
(UniProt - OMIM)
ITGA2B
(UniProt - OMIM)
ITGB3
(UniProt - OMIM)

INTERACTOME
ASSOCIATIONS
(click on a score value to see the evidence)
ITGA2B
ITGB3
(0.52)
(0.52)
FGA
FGA


Citations in the biomedical literature:


Fetal and neonatal alloimmune thrombocytopenia
CD109 GP1BA GP1BB ITGA2 ITGA2B ITGB3

Familial renal amyloidosis due to fibrinogen A alpha-chain variant
FGA



Fetal and neonatal alloimmune thrombocytopenia
Familial renal amyloidosis due to fibrinogen A alpha-chain variant

Synonym(s):
- NAIT
Synonym(s):
- Familial amyloid nephropathy due to fibrinogen A alpha-chain variant
- Fibrinogen A alpha-chain amyloidosis
- Hereditary amyloid nephropathy due to fibrinogen A alpha-chain variant
- Hereditary renal amyloidosis due to fibrinogen A alpha-chain variant
Classification (Orphanet):
- Rare hematologic disease
Classification (Orphanet):
- Rare genetic disease
- Rare renal disease
Classification (ICD10):
- Certain conditions originating in the perinatal period -
Classification (ICD10):
- Endocrine, nutritional and metabolic diseases -
Epidemiological data:
(no data available)
Epidemiological data:
(no data available)
External references:
No OMIM references
No MeSH references
External references:
No OMIM references
No MeSH references
No signs/symptoms info available.